Antibiotic susceptibility of Stenotrophomonas (Xanthomonas) maltophilia:: Comparative (NCCLS criteria) evaluation of antimicrobial drugs with the agar dilution and the agar disk diffusion (Bauer-Kirby) tests

被引:17
作者
Traub, WH [1 ]
Leonhard, B [1 ]
Bauer, D [1 ]
机构
[1] Univ Saarland, Inst Med Mikrobiol & Hyg, D-66421 Homburg, Germany
关键词
agar dilution test; agar disk diffusion (Bauer-Kirby) test; comparative evaluation; interpretative (NCCLS) criteria; minimal inhibitory concentrations; modified criteria (intermediate susceptibility); susceptibility;
D O I
10.1159/000007111
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ninety-six clinical isolates of Stenotrophomonas maltophilia were examined with the agar dilution method for susceptibility to 19 antimicrobial drugs. Doxycycline, cotrimoxazole, timentin, ofloxacin, fosfomycin, and piperacillin + tazobactam, in that order, inhibited the majority of strains. All isolates were resistant to nitrofurantoin. Concurrent disk susceptibility (Bauer-Kirby method) testing, using currently valid NCCLS interpretative criteria for Pseudomonas aeruginosa, uncovered a significant incidence of very major (category I), major (category II), and minor (categories III and IV) discrepancies for aminoglycosides, cephalosporins, chloramphenicol, and piperacillin + tazobactam and ticarcillin + clavulanic acid. Therefore, new interpretative criteria indicative of intermediate (I) susceptibility of S. maltophilia to these various antibiotics were proposed. In addition, new intermediate susceptibility criteria were proposed for the two beta-lactam-beta-lactamase inhibitor combinations. It was recommended to exclude ciprofloxacin from test batteries against this microorganism due to the wide scatter of minimal inhibitory concentration values and diameters of inhibition zones; the same was true for polymyxin B. It is hoped that the proposed modified, species-specific criteria will improve the clinical utility of laboratory-generated disk antibiograms with respect to the inherently multiple antibiotic-resistant, opportunistic pathogen S. maltophilia.
引用
收藏
页码:164 / 173
页数:10
相关论文
共 71 条
[21]   Stenotrophomonas maltophilia: Emergence of multidrug-resistant strains during therapy and in an in vitro pharmacodynamic chamber model [J].
Garrison, MW ;
Anderson, DE ;
Campbell, DM ;
Carroll, KC ;
Malone, CL ;
Anderson, JD ;
Hollis, RJ ;
Pfaller, MA .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (12) :2859-2864
[22]   DIVERSITY OF NOSOCOMIAL XANTHOMONAS-MALTOPHILIA (STENOTROPHOMONAS-MALTOPHILIA) AS DETERMINED BY RIBOTYPING [J].
GERNERSMIDT, P ;
BRUUN, B ;
ARPI, M ;
SCHMIDT, J .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1995, 14 (02) :137-140
[23]   ISOLATION OF A 30 KDA IMMUNOGLOBULIN BINDING-PROTEIN FROM PSEUDOMONAS-MALTOPHILIA [J].
GROVER, S ;
MCGEE, ZA ;
ODELL, WD .
JOURNAL OF IMMUNOLOGICAL METHODS, 1991, 141 (02) :187-197
[24]  
Gutiérrez F, 1996, CLIN INFECT DIS, V23, P1261, DOI 10.1093/clinids/23.6.1261
[25]   EFFECT OF DIVALENT-CATIONS IN BACTERIOLOGICAL MEDIA ON THE SUSCEPTIBILITY OF XANTHOMONAS-MALTOPHILIA TO IMIPENEM, WITH SPECIAL REFERENCE TO ZINC IONS [J].
HAWKEY, PM ;
BIRKENHEAD, D ;
KERR, KG ;
NEWTON, KE ;
HYDE, WA .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1993, 31 (01) :47-55
[26]   PNEUMONIA CAUSED BY STENOTROPHOMONAS-MALTOPHILIA WITH A MUCOID PHENOTYPE [J].
IRIFUNE, K ;
ISHIDA, T ;
SHIMOGUCHI, K ;
OHTAKE, J ;
TANAKA, T ;
MORIKAWA, N ;
KAKU, M ;
KOGA, H ;
KOHNO, S ;
HARA, K .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (11) :2856-2857
[27]   Adhesion of the positively charged bacterium Stenotrophomonas (Xanthomonas) maltophilia 70401 to glass and teflon [J].
Jucker, BA ;
Harms, H ;
Zehnder, AJB .
JOURNAL OF BACTERIOLOGY, 1996, 178 (18) :5472-5479
[28]  
KERR KG, 1991, REV INFECT DIS, V13, P762
[29]   A new selective differential medium for isolation of Stenotrophomonas maltophilia [J].
Kerr, KG ;
Denton, M ;
Todd, N ;
Corps, CM ;
Kumari, P ;
Hawkey, PM .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (07) :607-610
[30]  
KHARDORI N, 1990, REV INFECT DIS, V12, P997